Clinical Project Manager

Mansfield, MA

Join an established leader in the medical device diagnostic arena. Great team environment, career growth and compensation package!


  • Independently manage clinical trials
  • Ensure clinical studies are monitored in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs, utilizing knowledge of the diagnostic area
  • Assist clinical sites with IRB submission / documentation, if needed
  • Lead cross-functional effort to summarize and present clinical study data
  • Utilize a working knowledge of GCP and SOPs to assure compliance with FDA regulations
  • Work cross-functionally with Regulatory Affairs and Quality Management
  • Develop other team members through mentoring and coaching in complex subjects


  • BS/BA in life science discipline or equivalent combination of education and experience
  • 10+ years of successful experience in related field and successful performance of responsibilities presented above
  • Experience in in vitro diagnostics a plus
  • Strong writing and presentation skills
  • Ability to travel, domestic and international, depending upon project need, periodically up to 30-50% in US; less than 10% internationally

Inquiries and resumes to: Kathy Provost at OR 978/952-6425

For more information, please visit

Feb, 27, 2020